drugset / Trial / NCT01958320

Early Treatment Versus Delayed Conservative Treatment of the Patent Ductus Arteriosus

NCT01958320

Phase 2 Completed 202 enrolled University of California, San Francisco
RandomizedParallel-groupSingle-blindTreatment

Summary

The primary goal of the trial is to compare two different Patent Ductus Arteriosus (PDA) treatment approaches: 1) an "early treatment" approach or 2) a "conservative" approach. For the purposes of the study infants will be enrolled if they are delivered before 28 weeks gestation and have a moderate/large PDA present at 5-7 days after birth. The hypothesis is: treatment of a moderate size patent ductus arteriosus (PDA) will decrease the time needed for assisted respiratory support, diuretic therapy, and gavage feeding assistance, in addition to decreasing the incidence of ductus ligations or need for future outpatient cardiology follow-up appointments. The investigators hypothesize that one or more of these benefits will occur without an increase in the time taken to achieve full enteral feedings or in the incidence of necrotizing enterocolitis (NEC) or spontaneous intestinal perforations (SIP).The investigators will be comparing the effectiveness of early pharmacologic treatment with a control group of conservatively managed infants who will only receive treatment if they meet specific criteria for "rescue treatment".

Timeline

Start
2013-12
Primary completion
2017-06
Completion
2017-06

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Acetaminophen Small molecule
Subject Ibuprofen Small molecule
Subject Indomethacin Small molecule